Canonical Allele Identifier: CA438732294

Gene: SEPSECS

Linked Data

• MyVariant Identifiers: chr4:g.25146429T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.25144807T>G , CM000666.2:g.25144807T>G	GRCh38
NC_000004.11:g.25146429T>G , CM000666.1:g.25146429T>G	GRCh37
NC_000004.10:g.24755527T>G	NCBI36
NG_028222.1:g.20776A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000382103.7:c.993A>C MANE Select	ENSP00000371535.2:p.Ser331=
ENST00000680581.1:c.993A>C	ENSP00000506483.1:p.Ser331=
ENST00000680824.1:n.2209A>C
ENST00000681071.1:n.1285A>C
ENST00000681341.1:n.2134A>C
ENST00000681948.1:c.1248A>C	ENSP00000505991.1:p.Ser416=
ENST00000358971.7:c.*791A>C	ENSP00000351857.3:n.*791A>C
ENST00000382103.6:c.993A>C	ENSP00000371535.2:p.Ser331=
ENST00000503150.1:c.275A>C
ENST00000505513.1:n.293A>C
ENST00000514585.5:c.*694A>C	ENSP00000421880.1:n.*694A>C
NM_016955.3:c.993A>C	NP_058651.3:p.Ser331=
XM_005248168.2:c.756A>C	XP_005248225.1:p.Ser252=
XM_006713965.2:c.813A>C	XP_006714028.1:p.Ser271=
XM_011513846.1:c.990A>C	XP_011512148.1:p.Ser330=
XM_011513847.1:c.960A>C	XP_011512149.1:p.Ser320=
XM_011513848.1:c.813A>C	XP_011512150.1:p.Ser271=
XM_011513846.2:c.990A>C	XP_011512148.1:p.Ser330=
XM_011513847.2:c.960A>C	XP_011512149.1:p.Ser320=
XM_017008277.1:c.1248A>C	XP_016863766.1:p.Ser416=
XM_017008278.1:c.570A>C	XP_016863767.1:p.Ser190=
NM_016955.4:c.993A>C MANE Select	NP_058651.3:p.Ser331=